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Retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study
BACKGROUND: To measure the retinal/choroidal thicknesses in the macular area of asymptomatic pediatric patients with sickle cell disease (SCD). METHODS: This cross-sectional cohort study included 40 children (79 eyes) with SCD and 19 control patients (36 eyes). All subjects underwent spectral-domain...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895628/ https://www.ncbi.nlm.nih.gov/pubmed/35246275 http://dx.doi.org/10.1186/s40942-021-00351-3 |
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author | Prazeres, Juliana Lucatto, Luiz Filipe Ferreira, Adriano Moraes, Nilva Braga, Josefina A. P. Lima, Luiz H. Regatieri, Caio Maia, Maurício |
author_facet | Prazeres, Juliana Lucatto, Luiz Filipe Ferreira, Adriano Moraes, Nilva Braga, Josefina A. P. Lima, Luiz H. Regatieri, Caio Maia, Maurício |
author_sort | Prazeres, Juliana |
collection | PubMed |
description | BACKGROUND: To measure the retinal/choroidal thicknesses in the macular area of asymptomatic pediatric patients with sickle cell disease (SCD). METHODS: This cross-sectional cohort study included 40 children (79 eyes) with SCD and 19 control patients (36 eyes). All subjects underwent spectral-domain optical coherence tomography (SD-OCT) with enhanced-depth imaging OCT. Generalized Estimating Equations (GEE) were applied to compare the outcomes between groups. P ≤ 0.05 was considered significant. RESULTS: The choroidal thickness in the macular area in the study subfields was significantly thinner in the SCD eyes compared with control eyes (subfoveal subfield and temporal parafoveal subfield, p < 0.0001; nasal parafoveal subfield, p < 0.0001 temporal perifoveal subfield, p < 0.0001; and nasal perifoveal subfield, p < 0.0001). The variations in the retinal thickness were not significant. CONCLUSION: EDI-OCT showed that the macular choroidal thickness is thinner in asymptomatic pediatric patients with SCD. |
format | Online Article Text |
id | pubmed-8895628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88956282022-03-10 Retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study Prazeres, Juliana Lucatto, Luiz Filipe Ferreira, Adriano Moraes, Nilva Braga, Josefina A. P. Lima, Luiz H. Regatieri, Caio Maia, Maurício Int J Retina Vitreous Original Article BACKGROUND: To measure the retinal/choroidal thicknesses in the macular area of asymptomatic pediatric patients with sickle cell disease (SCD). METHODS: This cross-sectional cohort study included 40 children (79 eyes) with SCD and 19 control patients (36 eyes). All subjects underwent spectral-domain optical coherence tomography (SD-OCT) with enhanced-depth imaging OCT. Generalized Estimating Equations (GEE) were applied to compare the outcomes between groups. P ≤ 0.05 was considered significant. RESULTS: The choroidal thickness in the macular area in the study subfields was significantly thinner in the SCD eyes compared with control eyes (subfoveal subfield and temporal parafoveal subfield, p < 0.0001; nasal parafoveal subfield, p < 0.0001 temporal perifoveal subfield, p < 0.0001; and nasal perifoveal subfield, p < 0.0001). The variations in the retinal thickness were not significant. CONCLUSION: EDI-OCT showed that the macular choroidal thickness is thinner in asymptomatic pediatric patients with SCD. BioMed Central 2022-03-04 /pmc/articles/PMC8895628/ /pubmed/35246275 http://dx.doi.org/10.1186/s40942-021-00351-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Original Article Prazeres, Juliana Lucatto, Luiz Filipe Ferreira, Adriano Moraes, Nilva Braga, Josefina A. P. Lima, Luiz H. Regatieri, Caio Maia, Maurício Retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study |
title | Retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study |
title_full | Retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study |
title_fullStr | Retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study |
title_full_unstemmed | Retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study |
title_short | Retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study |
title_sort | retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895628/ https://www.ncbi.nlm.nih.gov/pubmed/35246275 http://dx.doi.org/10.1186/s40942-021-00351-3 |
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